HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Butanal → N-butyl-4-(4-fluorophenoxy)aniline
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Butanal | HCID 261 | — |
| Edukt | Benzenamine, 4-(4-fluorophenoxy)- | HCID 147633 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | N-butyl-4-(4-fluorophenoxy)aniline | HCID 71086302 | 62,7% |
Reaktionsschritte
To a solution of 4-(4-fluorophenoxy)aniline (Apollo, 500 mg, 2.46 mmol) and butyraldehyde (240 μL, 2.71 mmol) in DCE (5.0 mL) were added 4 Å molecular sieves. The resulting reaction mixture was stirred at room temperature for 1 h. Next, Na(OAc)3BH (782 mg, 3.69 mmol) was added, and the reaction mixture was stirred at room temperature overnight. Concentration in vacuo afforded a crude residue which was purified by flash column chromatography (10% EtOAc/hexanes) to give the title compound (400 mg, 62%). 1H NMR (CDCl3) δ 7.28-7.21 (m, 2H), 7.20-7.13 (m, 4H), 6.91-6.85 (m, 2H), 3.82 (br s, 1H), 3.39 (t, J=7.0 Hz, 2H), 1.96-1.85 (m, 2H), 1.79-1.67 (m, 2H), 1.26 (t, J=7.4 Hz, 3H); MS(ESI+) m/z 260.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09346795B2 |
| Quelldatensatz | uspto-grants-2016_05 |
| ORD ID | ord-e402595823f047f3ab20ee2c6fba20af |
| Quellennotiz | uspto-grants-2016_05 |